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3-(TRIFLUOROACETYL)INDOLE

3-(TRIFLUOROACETYL)INDOLE Structure
3-(TRIFLUOROACETYL)INDOLE
  • CAS No.14618-45-2
  • Chemical Name:3-(TRIFLUOROACETYL)INDOLE
  • CBNumber:CB5129548
  • Molecular Formula:C10H6F3NO
  • Formula Weight:213.16
  • MOL File:14618-45-2.mol
3-(TRIFLUOROACETYL)INDOLE Property
  • Melting point 211-214 °C(lit.)
  • Boiling point 308.6±37.0 °C(Predicted)
  • Density 1.423±0.06 g/cm3(Predicted)
  • storage temp. Sealed in dry,Room Temperature
  • pka 14.31±0.30(Predicted)
  • form Solid
  • color White to Almost white
  • CAS DataBase Reference 14618-45-2(CAS DataBase Reference)
  • UNSPSC Code 12352100
Safety
  • Hazard Codes  :Xi
  • Risk Statements  :36/37/38
  • Safety Statements  :26-36
  • WGK Germany  :3
  • HazardClass  :IRRITANT
  • HS Code  :2933992000
  • NFPA 704:
    0
    2 0
Hazard and Precautionary Statements (GHS)
  • Symbol(GHS)
  • Signal wordWarning
  • Hazard statements H315-H319-H335
  • Precautionary statements P261-P280a-P304+P340-P305+P351+P338-P405-P501a
3-(TRIFLUOROACETYL)INDOLE Price More Price(2)
  • Brand: TCI Chemicals (India)
  • Product number: T1809
  • Product name : 3-(Trifluoroacetyl)indole
  • Purity: min. 98.0 %
  • Packaging: 1G
  • Price: ₹5100
  • Updated: 2022/05/26
  • Buy: Buy
  • Brand: TCI Chemicals (India)
  • Product number: T1809
  • Product name : 3-(Trifluoroacetyl)indole
  • Purity: min. 98.0 %
  • Packaging: 5G
  • Price: ₹14700
  • Updated: 2022/05/26
  • Buy: Buy

3-(TRIFLUOROACETYL)INDOLE Chemical Properties,Usage,Production

  • Uses Reactant for enantioselective synthesis of indoles via palladium-catalyzed kinetic asymmetrical alkylation. Reactant for preparation of N-pyridinyl indolecarboxamides via amidation of aminopyridine derivatives. with indolecarboxylic acid 2 Reactant for preparation of mast cell tryptase inhibitors, starting from indoles; using amidation as the key step 3 Reactant for formation of Michael adducts via Baylis-Hillman reaction 4 Reactant for preparation of indolecarboxamides via haloform cleavage of (trifluoroacetyl)indole with lithium dialkylamides.
  • Uses
    • Reactant for enantioselective synthesis of indoles via palladium-catalyzed kinetic asymmetrical alkylation
    • Reactant for preparation of N-pyridinyl indolecarboxamides via amidation of aminopyridine derivatives. with indolecarboxylic acid
    • Reactant for preparation of mast cell tryptase inhibitors, starting from indoles; using amidation as the key step
    • Reactant for formation of Michael adducts via Baylis-Hillman reaction
    • Reactant for preparation of indolecarboxamides via haloform cleavage of (trifluoroacetyl)indole with lithium dialkylamides
  • General Description 3-(Trifluoroacetyl)indole is a heterocyclic trifluoromethyl ketone. One of the methods reported for its synthesis is by the reaction of indole with trifluoroacetic anhydride.
3-(TRIFLUOROACETYL)INDOLE Preparation Products And Raw materials
Raw materials
Preparation Products
3-(TRIFLUOROACETYL)INDOLE Suppliers
Global(91)Suppliers
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3-(TRIFLUOROACETYL)INDOLE Spectrum
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